US10961407B2 - Solvent-UV hybrid inkjet ink for aluminum beverage can decoration - Google Patents
Solvent-UV hybrid inkjet ink for aluminum beverage can decoration Download PDFInfo
- Publication number
- US10961407B2 US10961407B2 US16/402,036 US201916402036A US10961407B2 US 10961407 B2 US10961407 B2 US 10961407B2 US 201916402036 A US201916402036 A US 201916402036A US 10961407 B2 US10961407 B2 US 10961407B2
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- US
- United States
- Prior art keywords
- inkjet ink
- image
- radiation
- hybrid
- hybrid inkjet
- Prior art date
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Links
- 229910052782 aluminium Inorganic materials 0.000 title claims abstract description 23
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title claims abstract description 23
- 238000005034 decoration Methods 0.000 title claims abstract description 15
- 235000013361 beverage Nutrition 0.000 title claims description 13
- 239000000758 substrate Substances 0.000 claims abstract description 14
- 239000000463 material Substances 0.000 claims abstract description 13
- 239000000178 monomer Substances 0.000 claims description 25
- 239000002904 solvent Substances 0.000 claims description 23
- 239000002966 varnish Substances 0.000 claims description 20
- 238000000034 method Methods 0.000 claims description 16
- 239000003086 colorant Substances 0.000 claims description 9
- 239000011347 resin Substances 0.000 claims description 9
- 229920005989 resin Polymers 0.000 claims description 9
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 6
- 125000001931 aliphatic group Chemical group 0.000 claims description 5
- 239000004814 polyurethane Substances 0.000 claims description 5
- 229920002635 polyurethane Polymers 0.000 claims description 5
- LAIJAUHBAWLPCO-UHFFFAOYSA-N (4-tert-butylcyclohexyl) prop-2-enoate Chemical compound CC(C)(C)C1CCC(OC(=O)C=C)CC1 LAIJAUHBAWLPCO-UHFFFAOYSA-N 0.000 claims description 4
- KUAUJXBLDYVELT-UHFFFAOYSA-N 2-[[2,2-dimethyl-3-(oxiran-2-ylmethoxy)propoxy]methyl]oxirane Chemical compound C1OC1COCC(C)(C)COCC1CO1 KUAUJXBLDYVELT-UHFFFAOYSA-N 0.000 claims description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 4
- 229920000728 polyester Polymers 0.000 claims description 4
- RZVINYQDSSQUKO-UHFFFAOYSA-N 2-phenoxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC1=CC=CC=C1 RZVINYQDSSQUKO-UHFFFAOYSA-N 0.000 claims description 3
- VOBUAPTXJKMNCT-UHFFFAOYSA-N 1-prop-2-enoyloxyhexyl prop-2-enoate Chemical group CCCCCC(OC(=O)C=C)OC(=O)C=C VOBUAPTXJKMNCT-UHFFFAOYSA-N 0.000 claims description 2
- 125000004386 diacrylate group Chemical group 0.000 claims description 2
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 claims description 2
- FSDNTQSJGHSJBG-UHFFFAOYSA-N piperidine-4-carbonitrile Chemical compound N#CC1CCNCC1 FSDNTQSJGHSJBG-UHFFFAOYSA-N 0.000 claims description 2
- 229920005862 polyol Polymers 0.000 claims description 2
- 150000003077 polyols Chemical class 0.000 claims description 2
- 239000008365 aqueous carrier Substances 0.000 claims 1
- 230000001678 irradiating effect Effects 0.000 claims 1
- 150000002118 epoxides Chemical class 0.000 abstract description 12
- 239000003960 organic solvent Substances 0.000 abstract description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 5
- 239000000976 ink Substances 0.000 description 62
- -1 glycol ethers Chemical class 0.000 description 21
- 238000000576 coating method Methods 0.000 description 20
- 239000002253 acid Substances 0.000 description 12
- 239000011248 coating agent Substances 0.000 description 11
- 239000002270 dispersing agent Substances 0.000 description 10
- 239000000203 mixture Substances 0.000 description 10
- 239000000126 substance Substances 0.000 description 10
- 239000010408 film Substances 0.000 description 9
- 230000008569 process Effects 0.000 description 9
- 230000035882 stress Effects 0.000 description 8
- 239000004593 Epoxy Substances 0.000 description 7
- 150000002148 esters Chemical class 0.000 description 7
- 238000007639 printing Methods 0.000 description 7
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 6
- 238000007641 inkjet printing Methods 0.000 description 6
- 238000009928 pasteurization Methods 0.000 description 6
- 239000000049 pigment Substances 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 5
- 230000008901 benefit Effects 0.000 description 4
- 238000001723 curing Methods 0.000 description 4
- 238000011068 loading method Methods 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000003607 modifier Substances 0.000 description 4
- 238000007645 offset printing Methods 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- 239000004971 Cross linker Substances 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 229920000058 polyacrylate Polymers 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- NVVZQXQBYZPMLJ-UHFFFAOYSA-N formaldehyde;naphthalene-1-sulfonic acid Chemical class O=C.C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 NVVZQXQBYZPMLJ-UHFFFAOYSA-N 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 150000002596 lactones Chemical class 0.000 description 2
- UPHWVVKYDQHTCF-UHFFFAOYSA-N octadecylazanium;acetate Chemical compound CC(O)=O.CCCCCCCCCCCCCCCCCCN UPHWVVKYDQHTCF-UHFFFAOYSA-N 0.000 description 2
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229920001281 polyalkylene Polymers 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000000935 solvent evaporation Methods 0.000 description 2
- 238000007655 standard test method Methods 0.000 description 2
- 230000008646 thermal stress Effects 0.000 description 2
- 239000012855 volatile organic compound Substances 0.000 description 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- PSGCQDPCAWOCSH-UHFFFAOYSA-N (4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl) prop-2-enoate Chemical compound C1CC2(C)C(OC(=O)C=C)CC1C2(C)C PSGCQDPCAWOCSH-UHFFFAOYSA-N 0.000 description 1
- BXGYYDRIMBPOMN-UHFFFAOYSA-N 2-(hydroxymethoxy)ethoxymethanol Chemical compound OCOCCOCO BXGYYDRIMBPOMN-UHFFFAOYSA-N 0.000 description 1
- 239000012958 Amine synergist Substances 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 238000010546 Norrish type I reaction Methods 0.000 description 1
- 238000010547 Norrish type II reaction Methods 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 229920006243 acrylic copolymer Polymers 0.000 description 1
- 239000002318 adhesion promoter Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000001311 chemical methods and process Methods 0.000 description 1
- 229950007046 chlorphentermine Drugs 0.000 description 1
- IPHJYJHJDIGARM-UHFFFAOYSA-M copper phthalocyaninesulfonic acid, dioctadecyldimethylammonium salt Chemical compound [Cu+2].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC.C=1C(S(=O)(=O)[O-])=CC=C(C(=NC2=NC(C3=CC=CC=C32)=N2)[N-]3)C=1C3=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 IPHJYJHJDIGARM-UHFFFAOYSA-M 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 238000002161 passivation Methods 0.000 description 1
- 238000009304 pastoral farming Methods 0.000 description 1
- 230000037361 pathway Effects 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000003504 photosensitizing agent Substances 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- 238000003847 radiation curing Methods 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000007142 ring opening reaction Methods 0.000 description 1
- 238000007761 roller coating Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- BTURAGWYSMTVOW-UHFFFAOYSA-M sodium dodecanoate Chemical compound [Na+].CCCCCCCCCCCC([O-])=O BTURAGWYSMTVOW-UHFFFAOYSA-M 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 229940082004 sodium laurate Drugs 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000001029 thermal curing Methods 0.000 description 1
- 239000003017 thermal stabilizer Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/10—Printing inks based on artificial resins
- C09D11/101—Inks specially adapted for printing processes involving curing by wave energy or particle radiation, e.g. with UV-curing following the printing
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/30—Inkjet printing inks
- C09D11/36—Inkjet printing inks based on non-aqueous solvents
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/0041—Digital printing on surfaces other than ordinary paper
- B41M5/0047—Digital printing on surfaces other than ordinary paper by ink-jet printing
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/0041—Digital printing on surfaces other than ordinary paper
- B41M5/0058—Digital printing on surfaces other than ordinary paper on metals and oxidised metal surfaces
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/0082—Digital printing on bodies of particular shapes
- B41M5/0088—Digital printing on bodies of particular shapes by ink-jet printing
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M7/00—After-treatment of prints, e.g. heating, irradiating, setting of the ink, protection of the printed stock
- B41M7/0081—After-treatment of prints, e.g. heating, irradiating, setting of the ink, protection of the printed stock using electromagnetic radiation or waves, e.g. ultraviolet radiation, electron beams
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M7/00—After-treatment of prints, e.g. heating, irradiating, setting of the ink, protection of the printed stock
- B41M7/009—After-treatment of prints, e.g. heating, irradiating, setting of the ink, protection of the printed stock using thermal means, e.g. infrared radiation, heat
Definitions
- This invention pertains to solvent-UV hybrid inkjet inks adapted for use in inkjet decoration of aluminum beverage cans, to decorative and clear coatings produced with such inks, and to aluminum beverage cans decorated with images applied with such inks.
- Inkjet printing is widely used for digitally applying images to various substrates, which may be two-dimensional or three-dimensional. Such printing is achieved using inkjet printers having one or more printheads with nozzles for jetting the ink onto the substrate.
- the printheads are typically mounted on a carriage that moves back and forth as the substrate is advanced to receive the ink.
- the printheads can also be maintained in a stationary position and the substrate moved past the printheads.
- inkjet inks are formulated either with solvent carriers or with UV curable inks so that they can dry or cure, respectively, by solvent evaporation or UV radiation curing.
- solvent-based inkjet inks can accept high pigment loadings and produce thinner, more flexible coatings than UV cured inks.
- UV-cured inkjet inks also have important advantages, including quick curing, low VOCs, and good chemical resistance.
- Solvent-based inkjet inks do have limitations. For example, they typically do not adhere well to nonporous substrates like metal. Also, the final cured solvent-based inkjet ink films typically do not have good solvent resistance.
- ink performance is assessed by successfully passing the following critical evaluation points: 1) image resolution and quality, 2) ink cohesion with an overprint varnish, and 3) ink adhesion to the aluminum can. This assessment occurs throughout the can-making process, before and after heat exposure (thermal stress), can necking (mechanical stress), and pasteurization (chemical stress).
- the two-piece metal decoration process is carried out by first printing images on the outside of the can followed by an immediate application of a coating on the surface of the entire can (first piece), which is cured by baking at temperatures of 180-215° C. for 3-5 minutes. After this, the can is run through another baking step to thermally cure an inside spray-coated epoxy film that forms a barrier between the aluminum and beverage to protect product integrity. The cans are then subjected to a necking process, which reduces the diameter of the top edge of the cylindrical can down to end specifications.
- the necked cans will also be subjected to chemical stress by pasteurization prior to beverage filling and lid closure (second piece of two piece can), where the cans are submersed in 1% detergent at about 80-95° C. for 10-15 minutes. Since coatings prepared using low viscosity inks have suffered when subjected to this pasteurization step, it is also very important to ensure that any alternative formulations are able to withstand the stress of this chemical process.
- acrylate-based UV curable ink One type of digital inkjet ink that has the potential to meet the above requirements is acrylate-based UV curable ink.
- This type of ink generally: a) has excellent weather- and light-fastness durability, b) can be formulated at a 100% solids level to produce good overall film hardness, and c) is highly chemically resistant when sufficiently crosslinked.
- jettable acrylate-based UV curable inks have not generally been adopted in the marketplace because: 1) they produce overly thick printed images that impede necking, and 2) adhesive and cohesive failures are often encountered after the pasteurization step.
- a solvent-based digital ink might be considered to address the film thickness issue. This type of ink is thermally cured by solvent evaporation, leaving behind about 12-30% solids, producing a much thinner film.
- solvent-based inks are also rejected in the marketplace due their poor weatherability, light-fastness, and chemical resistance, and their high VOC content.
- solvent-based digital inks produce poor image quality compared to UV curable inks in metal can decorating applications.
- Embodiments of the present invention provide unique advances in digital printing on aluminum beverage cans using inkjet technology. These unique embodiments successfully pass the critical evaluation points and maintain high image quality and performance under duress from thermal stress due to oven baking and curing, mechanical stress due to can necking, and chemical stress due to pasteurization, and thus comprise a very significant contribution to the art.
- Embodiments of the present invention overcome the drawbacks of both acrylate-based UV curable and solvent-based inks by providing jettable low viscosity inkjet inks comprising a unique hybrid of UV-curable and solvent-based inks. These embodiments have highly desirable properties and advantages including: a) excellent weather- and light-fastness durability, b) ability to form thin films that can be formulated to a range of desired thicknesses, and c) excellent chemical resistance.
- Another important characteristic of embodiments is the ability to control step-wise cure.
- the printed image is UV-irradiated first, the resulting semi-cured film becomes immobile (pinned), yet is still wet due to the presence of unevaporated solvent.
- an overprint varnish by, e.g., an industry conventional roller coating process, intermixing of ink materials with overprint varnish components is achieved.
- This new ink-varnish composite produces a strong cohesion layer between the ink and varnish after the final thermal curing.
- overprint varnishes can be used.
- the overprint varnish preferably will include a solvent which may be either aqueous or organic.
- strong adhesion of the ink-varnish composite to aluminum cans may be enhanced by adding to the hybrid ink a third component that contains an epoxide functional group.
- a third component that contains an epoxide functional group By adding an epoxide-containing component to the hybrid ink and exposing the ink to high temperatures, the strain energy of the epoxide cyclic three-membered ring is released.
- application of elevated temperatures during the heat phase of the curing process is believed to catalyze the ring to break it open and covalently bind the ink to the aluminum surface.
- Hybrid inkjet ink embodiments of the present invention include, as necessary ingredients, about 3-49% by weight organic solvent based on the total weight of the ink, about 3-80% by weight of a UV radiation-curable material and an appropriate photoinitiator based on the total weight of the ink, and about 1-30% by weight of an epoxide-containing material based on the total weight of the ink.
- the organic solvent must be water miscible and preferably is food grade for applications to beverage cans.
- the organic solvent may be chosen from the group comprising of carbonates, lactones, glycols, and glycol ethers. Among these, lactones are currently preferred.
- the miscibility of the organic solvent with water based on weight percent ratio of organic solvent to water should be between about 95:5 and 5:95, and preferably between about 40:60 and 60:40.
- the UV radiation curable material may be chosen from one or more of a monofunctional UV curable monomer, a difunctional UV curable monomer or a trifunctional UV curable monomer.
- the UV curable component can contain two or more of a monofunctional UV curable monomer, a difunctional UV curable monomer or a trifunctional UV curable monomer.
- a mixture of all three of a monofunctional UV curable monomer, a difunctional UV curable monomer and a trifunctional UV curable monomer may be used.
- the monofunctional UV curable monomer may be a cycloaliphatic acrylate.
- Preferred cycloaliphatic acrylates include isobornyl acrylate and a most preferred cycloaliphatic acrylate is 4-tert-butylcyclohexylacrylate.
- Difunctional UV curable monomers When a difunctional UV curable monomer is used, it will act as a crosslinker. Difunctional monomers improve the hardness and chemical resistance of the film, as well as accelerate the rate of polymerization. Difunctional UV curable monomers that can be used include aliphatic, cycloaliphatic, polyester, polyurethane, and ethylene/propylene glycol diacrylates. Hexanediol diacrylate is preferred in embodiments and a most preferred difunctional UV curable monomer is dipropylene glycol diacrylate.
- Trifunctional UV curable monomer When a trifunctional UV curable monomer is used, it will also act as a crosslinker.
- One particularly preferred trifunctional UV curable monomer is propoxylated(3) trimethylopropane triacrylate. Trifunctional monomers provide harder films and a faster curing response with lower UV dosages.
- the UV curable component may also contain a resin to act as an adhesion promoter and/or to improve the hardness of the final coating.
- the resin may be, for example, one or more of a polyol, an acrylated polyester, or an acrylated polyurethane.
- the resin may be UV-radiation curable or it may not be UV-radiation curable.
- the molecular weights of the resin preferably will be less than about 100,000 Daltons, and most preferably will be in the range of about 1000-50,000 Daltons.
- composition will also include epoxy functional modifiers and photoinitiators that act as polymerization initiators.
- the epoxide containing material will be a mono-, di-, or tri-functional epoxide chosen from the group comprising aliphatic, aromatic, saturated and unsaturated epoxides. Among these, aliphatic epoxides are currently preferred. As explained earlier, the epoxide containing material is believed to act as cross-linkers and to improve the adhesion to metal oxide surfaces, such as the aluminum oxide found in the surface of aluminum cans.
- the epoxy containing material may comprise mono- or di-epoxy containing monomers.
- Preferred epoxy functional modifiers include cyclohexyl dimethanol diglycidyl ether. A particularly preferred epoxy functional modifier is neopentyl glycol diglycidyl ether.
- the inkjet ink composition may be used as a colorant-free clear coating or varnish, in most applications it will include a colorant, which can be pretreated so that it is self-dispersing or it may include a colorant in the form of a pigment or dye in combination with a separate dispersant. In the latter case the colorant will be stabilized using appropriate dispersants that are compatible with the UV curable component, the epoxy functional modifier, and the solvent.
- One measure of compatibility is that the combined components in the ink must be stable at elevated temperatures, broadly from about 20-80° C. for four weeks, and preferably from about 20-60° C. for two weeks.
- a dispersant is preferably added not only to improve the dispersibility of the colorant (when needed) but also to improve the storage stability of the ink.
- examples of dispersants that can be used include hydroxyl group-containing carboxylate esters, salts of long-chain polyaminoamides and esters of high molecular weight acids, salts of high molecular weight polycarboxylic acids, salts of long-chain polyaminoamides and esters of polar acids, esters of high molecular weight unsaturated acids, high molecular weight copolymers, modified polyurethanes, modified polyacrylates, polyetherester-based anionic surfactants, salts of naphthalenesulfonic acid-formalin condensation products, salts of aromatic sulfonic acid-formalin condensation products, polyoxyethylene alkylphosphate esters, polyoxyethylene nonylphenyl ether, and stearylamine acetate.
- suitable dispersants include “Anti-Terra-U (a polyaminoamide phosphate)”, “Anti-Terra-203/204 (salts of high molecular weight polycarboxylic acids)”, “Disperbyk-101 (a phosphate salt of a polyaminoamide and an acid ester), 107 (a hydroxyl group-containing carboxylate ester), 110 and 111 (copolymers that contain acid groups), 130 (a polya-25 mide), 161,162, 163,164, 165, 166 and 170 (high molecular weight copolymers)”, “Bykumen (an ester of a high molecular weight unsaturated acid)”, “BYK-P104, P105 (high molecular weight unsaturated polycarboxylic acids”, “P104S, 240S (systems containing a high molecular weight unsaturated polycarboxylic acid and silicon)”, and “Lactimon (a combination of a long-chain amine, an unsaturated polycarboxylic acids
- Still other suitable dispersants include “Demol RN and N (sodium salts of naphthalene-sulfonic acid-formalin condensates), MS, C and SN-B (sodium salts of aromatic sulfonic acid-formalin condensates), and EP”, “Homogenol L-18 (a polycarboxylic acid type polymer)”, “Emalgen 920, 930, 931,935,950 and 985 (polyoxy-ethylene nonylphenyl ethers)”, and “Acetamine 24 (a coconut amine acetate) and 86 (stearylamine acetate)” (Kao Corporation) “Solsperse 5000 (a phthalocyanine ammonium salt system), 13940 (a polyes-teramine system), 17000 (a fatty acid amine system), and 24000” (Avecia Ltd.) “Nikol T106 (a polyoxyethylene sorbitan monooleate) and MYS-IEX (a polyoxy
- the inkjet ink composition will also include conventional ingredients like colorants, photosensitizers, photosynergists, stabilizers and surfactants.
- surfactants examples include fluorosurfactants, anionic surfactants such as sodium dodecylbenzenesulfonate, sodium laurate, and ammonium salts of polyoxyethylene alkyl ether sulfate; and nonionic surfactants such as polyoxy-ethylene alkyl ethers, polyoxyethylene alkyl esters, polyoxy-25 ethylene sorbitan fatty acid esters, polyoxyethylene alkylphenyl ethers, polyoxyethylene alkylamines, and polyoxyethylene alkylamides.
- Other examples of surfactants that can be used include polyoxyalkylene polyalkylene amines and sorbitan esters.
- polyoxyalkylene polyalkylene polyamines examples include Discole N-503, N-506, N-509, N-512, N-515, N-518, and N-520. (Dainichiseika Coln and Chemicals Mfg. Co.)
- Printed decorations prepared using the inkjet composition of embodiments will have a film thickness of about 1 to 12 ⁇ m, preferably about 1-10 ⁇ m and most preferably about 1-8 ⁇ m. These ink thicknesses enable the coating to successfully withstand mechanical stress put on the can container by the necking machinery.
- the coatings, in their final cured state will have a pencil hardness between 3B to 9H, and preferably between 2B to 9H.
- an overprint varnish will be applied to coatings prepared using the inkjet printing compositions.
- Overprint varnishes are used to help protect ink coatings.
- the level of protection and enhanced image quality achieved by intermixing the overprint varnish and the hybrid ink embodiments is outstanding.
- processes to produce decorative coatings in accordance with embodiments will entail: A) application of the inkjet composition using an inkjet printer followed by UV irradiation to achieve a partial cure; B) application of the overprint coating and, C) final heating to produce full cure.
- the UV curable component is initially pinned by applying UV radiation to cure (polymerize) that component, leaving the unevaporated solvent of the hybrid ink in place and an interim coating in the form of a “semi-wet print”.
- the overprint coating is applied to the “semi-wet print” it intermixes with the water miscible solvent component before the final heating step. While heating times and temperatures may vary depending on system parameters, the heating following the initial application may be carried out in an oven, for example, at about 80-350° C. for about 1-40 minutes, and most preferably about 180-215° C. for about 3-5 minutes.
- the outstanding adhesion image quality, glossiness and other properties achieved may be obtained when the aluminum oxide passivation layer formed on the surface of the can container during the heating step reacts with the oxygen in the epoxide group of the epoxide-containing component to initiate reaction with other components in the ink composition.
- the Al 3+ ion species on the surface of the can is coordinated by the epoxide oxygen, catalyzing a ring-opening and reaction with other components of the ink.
- test specimens were successfully necked cans with inkjet-applied decoration and an overprint varnish top coat.
- An ASTM standard test method D3359-09 was used to measure and examine the adhesion of inkjet-applied hybrid ink.
- a hard metal straight edge was used to make straight cuts with a sharp razor blade to form intersecting 7 to 8 crosshatched cuts in selected areas of the body and neck of the cans.
- the tape applied was a 0.75′′ wide transparent Scotch® Brand Tape, Cat 600.
- An ASTM standard test method D523-08 was used to measure the specular gloss of nonmetallic specimens for glossmeter geometries of 20, 60, and 85° using two specimens: 1) a hybrid black ink prepared in accordance with embodiments of the invention and applied using an inkjet printer, and 2) a commercial black beverage can coating prepared using conventional offset printing.
- a black hybrid inkjet ink as follows was used:
- the 20° geometry is advantageous for comparing specimens having 60° gloss values higher than 70.
- the 60° geometry is used for inter-comparing most specimens and for determining when the 20° geometry may be more applicable.
- the 85° geometry is used for comparing specimens for sheen or near-grazing shininess; it is most frequently applied when specimens have 60° gloss values lower than 10.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Ink Jet Recording Methods And Recording Media Thereof (AREA)
- Other Surface Treatments For Metallic Materials (AREA)
- Ink Jet (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Manufacturing & Machinery (AREA)
Abstract
Description
Material Type | Percent by Weight |
4-tert-butylcyclohexyl acrylate (monomer) | 13 |
2-phenoxyethyl acrylate (monomer) | 4 |
Propoxylated (3) Trimethylopropane Triacrylate | 6 |
(trifunctional monomer) | |
Resin | 12 |
Amine Synergist | 8 |
Antioxidant and thermal stabilizer blend | 1 |
Surfactant | 1 |
Photoinitiator Norrish Type I | 3.5 |
Photoinitiator Norrish Type II | 3.5 |
Black Pigment Dispersion (colorant) | 15 |
Gamma-butyrolactone (solvent) | 20 |
Neopentyl glycol diglycidyl ether (epoxide) | 13 |
100 | |
Gloss Level |
Commercial | Hybrid | |
Angle | Black | Black |
20° | 57.6 | 66.7 |
60° | 87.4 | 89.9 |
85° | 96.6 | 94.4 |
Claims (14)
Priority Applications (1)
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US16/402,036 US10961407B2 (en) | 2016-04-13 | 2019-05-02 | Solvent-UV hybrid inkjet ink for aluminum beverage can decoration |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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US201662322007P | 2016-04-13 | 2016-04-13 | |
US15/229,557 US20170298240A1 (en) | 2016-04-13 | 2016-08-05 | Solvent-uv hybrid inkjet ink for aluminum beverage can decoration |
US16/402,036 US10961407B2 (en) | 2016-04-13 | 2019-05-02 | Solvent-UV hybrid inkjet ink for aluminum beverage can decoration |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US15/229,557 Continuation US20170298240A1 (en) | 2016-04-13 | 2016-08-05 | Solvent-uv hybrid inkjet ink for aluminum beverage can decoration |
Publications (2)
Publication Number | Publication Date |
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US20200095436A1 US20200095436A1 (en) | 2020-03-26 |
US10961407B2 true US10961407B2 (en) | 2021-03-30 |
Family
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US15/229,557 Abandoned US20170298240A1 (en) | 2016-04-13 | 2016-08-05 | Solvent-uv hybrid inkjet ink for aluminum beverage can decoration |
US16/402,036 Active US10961407B2 (en) | 2016-04-13 | 2019-05-02 | Solvent-UV hybrid inkjet ink for aluminum beverage can decoration |
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US15/229,557 Abandoned US20170298240A1 (en) | 2016-04-13 | 2016-08-05 | Solvent-uv hybrid inkjet ink for aluminum beverage can decoration |
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US (2) | US20170298240A1 (en) |
EP (1) | EP3426738A4 (en) |
JP (1) | JP7049999B2 (en) |
WO (1) | WO2017180637A1 (en) |
Families Citing this family (6)
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GB201620917D0 (en) * | 2016-12-08 | 2017-01-25 | Crown Packaging Technology Inc | Forming a texture in a can surface decoration |
US10677621B1 (en) | 2017-09-20 | 2020-06-09 | Continental Control Systems Llc | Sensor apparatus for two-wire sensor measurement and information read-out system |
AU2019260829A1 (en) * | 2018-04-27 | 2020-11-26 | Juno Dts, Llc | System and method for printing on a treated surface |
US20200269623A1 (en) * | 2019-02-22 | 2020-08-27 | Xyrec Ip B.V. | Methods of printing on non-permeable surfaces |
US11383545B2 (en) * | 2019-05-01 | 2022-07-12 | Xerox Corporation | Apparatus and method for deposting an overcoat on an image on a substrate |
US11639064B2 (en) | 2020-10-23 | 2023-05-02 | Ricoh Company, Ltd. | Image forming method |
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Also Published As
Publication number | Publication date |
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JP7049999B2 (en) | 2022-04-07 |
WO2017180637A1 (en) | 2017-10-19 |
US20200095436A1 (en) | 2020-03-26 |
EP3426738A4 (en) | 2019-12-04 |
JP2019518812A (en) | 2019-07-04 |
US20170298240A1 (en) | 2017-10-19 |
EP3426738A1 (en) | 2019-01-16 |
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